FADD

mutation — cross-omics
Cross-omicsMUTATION → PROTEIN-RPPAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, FADD mutation is significantly associated with the total protein of many other genes, with 9 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FADD-associated genes across cancer lineages are EGFR_pY1068, S6_pS240_S244, and VHL. Each is linked with FADD in more than 1 cancer types. Because this analysis shows association rather than direction, both FADD-to-partner and partner-to-FADD results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, EGFR_pY1068 grouped by FADD-low versus FADD-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FADD→partner) and Y-score (partner→FADD) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
UCECEGFR_pY1068 →-0.352-3.000.015.03731
UCECS6_pS240_S244 →+0.487+3.000.038.03731
UCECVHL →-1.286-3.000.001.03731
UCECDi-Ras3 →-0.246-3.000.004.03721
UCECAcetyl-a-Tubulin-Lys40 →+0.751+3.000.010.03711
UCECRab25 →-0.378-3.000.048.03711
Each partner links to its Q-omics profile. Showing the 6 strongest of 9 associations by consensus.

EGFR_pY1068 by FADD expression — UCEC

Box plot of EGFR_pY1068 in FADD-low vs FADD-high samples in UCEC.

Explore this box plot interactively →

Exploration